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Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness
Interethnic variability in drug response arises from genetic differences associated with drug metabolism, action and transport. These genetic variations can affect drug efficacy as well as cause adverse drug reactions (ADRs). We retrieved drug-response related single nucleotide polymorphism (SNP) as...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977754/ https://www.ncbi.nlm.nih.gov/pubmed/31971968 http://dx.doi.org/10.1371/journal.pone.0228000 |
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author | Ahsan, Tamim Urmi, Nusrat Jahan Sajib, Abu Ashfaqur |
author_facet | Ahsan, Tamim Urmi, Nusrat Jahan Sajib, Abu Ashfaqur |
author_sort | Ahsan, Tamim |
collection | PubMed |
description | Interethnic variability in drug response arises from genetic differences associated with drug metabolism, action and transport. These genetic variations can affect drug efficacy as well as cause adverse drug reactions (ADRs). We retrieved drug-response related single nucleotide polymorphism (SNP) associated data from databases and analyzed to elucidate population specific distribution of 159 drug-response related SNPs in twenty six populations belonging to five super-populations (African, Admixed Americans, East Asian, European and South Asian). Significant interpopulation differences exist in the minor (variant) allele frequencies (MAFs), linkage disequilibrium (LD) and haplotype distributions among these populations. 65 of the drug-response related alleles, which are considered as minor (variant) in global population, are present as the major alleles (frequency ≥0.5) in at least one or more populations. Populations that belong to the same super-population have similar distribution pattern for majority of the variant alleles. These drug response related variant allele frequencies and their pairwise LD measure (r(2)) can clearly distinguish the populations in a way that correspond to the known evolutionary history of human and current geographic distributions, while D' cannot. The data presented here may aid in identifying drugs that are more appropriate and/or require pharmacogenetic testing in these populations. Our findings emphasize on the importance of distinct, ethnicity-specific clinical guidelines, especially for the African populations, to avoid ADRs and ensure effective drug treatment. |
format | Online Article Text |
id | pubmed-6977754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69777542020-02-07 Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness Ahsan, Tamim Urmi, Nusrat Jahan Sajib, Abu Ashfaqur PLoS One Research Article Interethnic variability in drug response arises from genetic differences associated with drug metabolism, action and transport. These genetic variations can affect drug efficacy as well as cause adverse drug reactions (ADRs). We retrieved drug-response related single nucleotide polymorphism (SNP) associated data from databases and analyzed to elucidate population specific distribution of 159 drug-response related SNPs in twenty six populations belonging to five super-populations (African, Admixed Americans, East Asian, European and South Asian). Significant interpopulation differences exist in the minor (variant) allele frequencies (MAFs), linkage disequilibrium (LD) and haplotype distributions among these populations. 65 of the drug-response related alleles, which are considered as minor (variant) in global population, are present as the major alleles (frequency ≥0.5) in at least one or more populations. Populations that belong to the same super-population have similar distribution pattern for majority of the variant alleles. These drug response related variant allele frequencies and their pairwise LD measure (r(2)) can clearly distinguish the populations in a way that correspond to the known evolutionary history of human and current geographic distributions, while D' cannot. The data presented here may aid in identifying drugs that are more appropriate and/or require pharmacogenetic testing in these populations. Our findings emphasize on the importance of distinct, ethnicity-specific clinical guidelines, especially for the African populations, to avoid ADRs and ensure effective drug treatment. Public Library of Science 2020-01-23 /pmc/articles/PMC6977754/ /pubmed/31971968 http://dx.doi.org/10.1371/journal.pone.0228000 Text en © 2020 Ahsan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ahsan, Tamim Urmi, Nusrat Jahan Sajib, Abu Ashfaqur Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title | Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title_full | Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title_fullStr | Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title_full_unstemmed | Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title_short | Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness |
title_sort | heterogeneity in the distribution of 159 drug-response related snps in world populations and their genetic relatedness |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977754/ https://www.ncbi.nlm.nih.gov/pubmed/31971968 http://dx.doi.org/10.1371/journal.pone.0228000 |
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